Teva Quality Assurance Analyst 

Greece, Peloponnese, Western Greece and the Ionian 

740823570

• Be the Commercial Quality business partner of Teva Pharmaceuticals Hellas S.A., to ensure products are efficiently distributed into the country by meeting Teva, regional and local standards and customer needs.
• Ensure market release from approved suppliers based on batch release documentation and transport conditions documentation; ensure GDP compliance of the distribution center(s); deciding on final disposition of rejected, recalled or falsified products.
• Ensure quality complaints are registered and liaise with manufacturing site to trigger corresponding investigation and adequate corrective actions.
• In case of recall ensure promptly local coordination between Pharmacovigilance, Medical Affairs, Regulatory Affairs, Supply Chain, etc. and with EU Qualified person concerned. Escalate any critical information to (sub regional) Head of Commercial Quality and issue the final recall report.
• Change control, deviations and CAPAs: Use validated computerized systems for change control, deviation and CAPA handling.
• Suppliers/customers and 3rd party service providers: Maintain and monitor a list of approved suppliers/customers/providers; ensure Quality Agreements are drawn up and kept updated with all local suppliers/customers and 3rd party service providers as required.
• Evaluate the local GxP impact for any future release and changes; assure the compliance of validated ERP system with GxP user requirements as per relevant local regulations.
• Support Teva and Quality strategic business Initiatives: assure the execution of sub-regional projects coordinated in the country, as applicable; support Sub-Regional/Regional Quality initiatives outside the country as needed.
• Ensure GDP compliance at the commercial unit and promote quality culture.
• Create, maintain up-to-date and distribute Standard Operating Procedures and Working Instructions as per Teva standard and in compliance with national regulations.
• Ensure initial and continuous GDP training implementation and maintenance at a local level.
• Attend to European monthly Quality Councils; provide the local monthly quality metrics to the European Commercial Quality; provide GxP guidance and quality oversight of local GxP business activities/deliverables.
• Initiate continuous improvement of processes.

• University degree in Pharmacy, Chemistry, Biology, Chemical Engineering or other relevant
• Postgraduate degree(s) in life–science and/or business administration would be highly preferable
• Proven work record of at least 1 year in Quality Assurance Affairs in Pharmaceutical (multinational or local) and/or Consulting Companies is preferred
• Knowledge in Quality Assurance topics will be considered an asset
• Demonstrated capability of being able to work concurrently on several projects, understand and evaluate complex information
• Knowledge in European and Greek pharmaceutical legislation, relevant guidelines, procedures and requirements
• Computer literate (Microsoft Outlook, Word, Excel; Acrobat Pro)
• Excellent verbal communication skills
• Ability to work under pressure and efficiently meet tight timelines
• Ability to organize, plan and prioritize work
• Capability to establish and maintain constructive interpersonal relationships
• Excellent command of Greek and English language (spoken and written)

• Dynamic working environment
• Competitive remuneration package
• Continuous learning & development opportunities

Please, kindly note that only shortlisted applicants will be contacted. All personal data is protected by law and will be treated in confidence.

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